Advances in Wearable Sensing Technologies and Their Impact for Personalized and Preventive Medicine

Recent advances in miniaturized electronics, as well as mobile access to computational power, are fostering a rapid growth of wearable technologies. In particular, the application of such wearable technologies to health care enables to access more information from the patient than standard episodically testing conducted in health provider centres. Clinical, behavioural and self-monitored data collected by wearable devices provide a means for improving the early-stage detection and management of diseases as well as reducing the overall costs over more invasive standard diagnostics approaches. In this chapter, we will discuss some of the ongoing key innovations in materials science and micro/nano-fabrication technologies that are setting the basis for future personalized and preventive medicine devices and approaches. The design of wire- and power-less ultra-thin sensors fabricated on wearable biocompatible materials that can be placed in direct contact with the body tissues such as the skin will be reviewed, focusing on emerging solutions and bottlenecks. The application of nanotechnology for the fabrication of sophisticated miniaturized sensors will be presented. Exemplary sensor designs for the non-invasive measurement of ultra-low concentrations of important biomarkers will be discussed as case studies for the application of these emerging technologies

Near-Infrared Active Lead Chalcogenide Quantum Dots: Preparation, Post-Synthesis Ligand Exchange, and lications in Solar Cells

Quantum dots (QDs) of lead chalcogenides (e.g. PbS, PbSe, and PbTe) are attractive near‐infrared (NIR) active materials that show great potential in a wide range of applications, such as, photovoltaics (PV), optoelectronics, sensors, and bio‐electronics. The surface ligand plays an essential role in the production of QDs, post‐synthesis modification, and their integration to practical applications. Therefore, it is critically important that the influence of surface ligands on the synthesis and properties of QDs is well understood for their applications in various devices. In this Review we elaborate the application of colloidal synthesis techniques for the preparation of lead chalcogenide based QDs. We specifically focus on the influence of surface ligands on the synthesis of QDs and their solution‐phase ligand exchange. Given the importance of lead chalcogenide QDs as potential light harvesters, we also pay particular attention to the current progress of these QDs in photovoltaic applications.This work was financially supported by the Australian Research Council Discovery Projects DP110102877 and DP140104062, DP150101939 and Discovery Early Career Award DE16010056

One-Step Rapid and Scalable Flame Synthesis of Efficient WO3 Photoanodes for Water Splitting

Photoelectrochemical water splitting is a promising approach for the carbon‐free production of hydrogen using sunlight. Here, robust and efficient WO3 photoanodes for water oxidation were synthesized by the scalable one‐step flame synthesis of nanoparticle aerosols and direct gas‐phase deposition. Nanostructured WO3 films with tunable thickness and band gap and controllable porosity were fabricated by controlling the aerosol deposition time, concentration, and temperature. Optimal WO3 films demonstrate superior water oxidation performance, reaching a current density of 0.91 mA at 1.24 V vs. reversible hydrogen electrode (RHE) and an incident photon‐to‐current conversion efficiency (IPCE) of ca. 61 % at 360 nm in 0.1 m H2SO4. Notably, it is found that the excellent performance of these WO3 nanostructures arises from the high in situ restructuring temperature (ca. 1000 °C), which increases oxygen vacancies and decreases charge recombination at the WO3/electrolyte interface. These findings provide a scalable approach for the fabrication of efficient photoelectrodes based on WO3 and other metal oxides for light‐driven water splitting.A.T. gratefully acknowledges the support of the Australian Research Council (AR; DP150101939, ARC DE160100569), and a Westpac 2016 Research Fellowship

Size-selected agglomerates of SnO₂ nanoparticles as gas sensors

The effect of nanoparticle structure on gas sensing performance is investigated. Size-selected nanostructured SnO₂ agglomerate particles for gas sensors were made by scalable flame spray pyrolysis. These particles were polydisperse (up to 12μm in diameter) and consisted of primary particles of 10nm in grain and crystal size as measured by transmission electron microscopy, x-ray diffraction, and Berner low pressure impactor (BLPI). The effect of agglomerate size on thermal stability and sensing of ethanol vapor (4–100ppm) and CO (4–50ppm) was investigated by selecting nearly monodisperse fractions of these agglomerates by the BLPI. Sensor layers made with these size-fractionated agglomerates exhibited higher thermal stability and dramatically enhanced sensitivity for both analytes than layers made with polydisperse agglomerates. This is attributed to their aggregate (or hard agglomerate) structure exhibiting small sinter necks between their constituent primary particles of tin dioxide that had also a narrow size distribution as expected for particles generated in flames. Upon further sintering of these optimally sized, nanostructured agglomerates, grain and neck growth degraded their superior sensitivity, supporting the proposed mechanism of their enhanced sensitivity: optimal primary particle necking.Financial support was provided by ETH Zurich FEL-04 08-3, Finnish Academy, Tekes The Finnish National Technology Agency, and Nanoprim

Blood-Flow-Restriction-Training-Induced Hormonal Response is not Associated with Gains in Muscle Size and Strength

The aim of this study was to determine whether increases in post-exercise endocrine response to low-load resistance exercise with blood flow restriction and high-load resistance exercise would have association with increases in muscle size and strength after an 8-week training period. Twenty-nine untrained men were randomly allocated into three groups: low-load resistance exercise with (LL-BFR) or without blood flow restriction (LL), and high-load resistance exercise (HL). Participants from LL-BFR and LL groups performed leg extension exercise at 20% of one repetition maximum (1RM), four sets of 15 repetitions and the HL group performed four sets of eight repetitions at 80% 1RM. Before the first training session, growth hormone (GH), insulin-like growth factor 1 (IGF-1), testosterone, cortisol, and lactate concentration were measured at rest and 15 min after the exercise. Quadriceps CSA and 1RM knee extension were assessed at baseline and after an 8-week training period. GH increased 15 min after exercise in the LL-BFR (p = 0.032) and HL (p \u3c 0.001) groups, with GH concentration in the HL group being higher than in the LL group (p = 0.010). There was a time effect for a decrease in testosterone (p = 0.042) and an increase in cortisol (p = 0.005), while IGF-1 remained unchanged (p = 0.346). Both muscle size and strength were increased after training in LL-BFR and HL groups, however, these changes were not associated with the acute post-exercise hormone levels (p \u3e 0.05). Our data suggest that other mechanisms than the acute post-exercise increase in systemic hormones induced by LL-BFR and HL produce changes in muscle size and strength

First Principles Analysis of H2O Adsorption on the (110) Surfaces of SnO2, TiO2 and Their Solid Solutions

Both associative and dissociative H2O adsorption on SnO2(110), TiO2(110), and Ti-enriched Sn1-xTixO2(110) surfaces have been investigated at low (1/12 monolayer (ML)) and high coverage (1 ML) by density functional theory calculations using the Gaussian and plane waves formalism. The use of a large supercell allowed the simulation at low symmetry levels. On SnO2(110), dissociative adsorption was favored at all coverages and was accompanied by stable associative H2O configurations. Increasing the coverage from 1/12 to 1 ML stabilized the (associatively or dissociatively) adsorbed H2O on SnO2(110) because of the formation of intermolecular H bonds. In contrast, on TiO2(110), the adsorption of isolated H2O groups (1/12 ML) was more stable than at high coverage, and the favored adsorption changed from dissociative to associative with increasing coverage. For dissociative H2O adsorption on Ti-enriched Sn1-xTixO2(110) surfaces with Ti atoms preferably located on 6-fold-coordinated surface sites, the analysis of the Wannier centers showed a polarization of electrons surrounding bridging O atoms that were bound simultaneously to 6-fold-coordinated Sn and Ti surface atoms. This polarization suggested the formation of an additional bond between the 6-fold-coordinated Ti-6c and bridging O atoms that had to be broken upon H2O adsorption. As a result, the H2O adsorption energy initially decreased, with increasing surface Ti content reaching a minimum at 25% Ti for 1/12 ML. This behavior was even more accentuated at high H2O coverage (1 ML) with the adsorption energy decreasing rapidly from 145.2 to 101.6 kJ/mol with the surface Ti content increasing from 0 to 33%. A global minimum of binding energies at both low and high coverage was found between 25 and 33% surface Ti content, which may explain the minimal cross-sensitivity to humidity previously reported for Sn1-xTixO2 gas sensors. Above 12.5% surface Ti content, the binding energy decreased with increasing coverage, suggesting that the partial desorption of H2O is facilitated at a high fractional coverage

Superior Self-Powered Room-Temperature Chemical Sensing with Light-Activated Inorganic Halides Perovskites

Hybrid halide perovskite is one of the promising light absorber and is intensively investigated for many optoelectronic applications. Here, the first prototype of a self-powered inorganic halides perovskite for chemical gas sensing at room temperature under visible-light irradiation is presented. These devices consist of porous network of CsPbBr3 (CPB) and can generate an open-circuit voltage of 0.87 V under visible-light irradiation, which can be used to detect various concentrations of O2 and parts per million concentrations of medically relevant volatile organic compounds such as acetone and ethanol with very quick response and recovery time. It is observed that O2 gas can passivate the surface trap sites in CPB and the ambipolar charge transport in the perovskite layer results in a distinct sensing mechanism compared with established semiconductors with symmetric electrical response to both oxidizing and reducing gases. The platform of CPB-based gas sensor provides new insights for the emerging area of wearable sensors for personalized and preventive medicine.H.C. and M.Z. contributed equally to this work. A.T. gratefully acknowledges the support of Australian Research Council (ARC) DP150101939, ARC DE160100569, and Westpac 2016 Research Fellowship. M.Z., S.H., and A.W.Y. H.-B. acknowledge the support of the Australian government via financial support from the ARC through the DP160102955 program and the Australian Renewable Energy Agency. K.R.C. acknowledges the support of an ARC Future Fellowship. The financial support from ARC through DP160102955 is also acknowledged

A graphene film interlayer for enhanced electrical conductivity in a carbon-fibre/PEEK composite

Carbon-fibre reinforced composites are seeing increased deployment, especially in the aerospace industry, and the next-generation of these materials will need to meet demanding performance requirements beyond just specific strength. The incorporation of nanomaterials such as graphene into composites has great potential for enhancing electrical, thermal, and mechanical properties, which could then enable new capabilities such as built-in lightning strike protection and electromagnetic shielding. One major challenge is successful integration of nanomaterials into the composite during the manufacturing process especially for thermoplastic based composites. This work explores the spray deposition of exfoliated graphene in liquid suspensions for the nano-enhancement of electrical properties in carbon-fibre reinforced polyether ether keytone (PEEK) composites. Developed thin films were smooth with RMS roughness of 1.06 μm on Si substrates and RMS roughness of 1.27 μm on CF-PEEK tapes. The addition of 1.3 wt% graphene into the interlayers of CF-PEEK composites resulted in bulk electrical conductivity enhancement both in plane and through thickness of ~ 1100% and 67.5% respectively. This approach allows for pre-consolidation introduction of high-performance nanomaterials directly to thermoplastic prepregs which could open simple pathways for the in-situ manufacturing of carbon-fibre reinforced polymer nanocomposites.This project was conducted within the ARC Training Centre for Automated Manufacture of Advanced Composites (IC160100040), supported by the Commonwealth of Australia under the Australian Research Council’s Industrial Transformation Research Program

Engineering of chitosan-hydroxyapatite-magnetite hierarchical scaffolds for guided bone growth

Bioabsorbable materials have received increasing attention as innovative systems for the development of osteoconductive biomaterials for bone tissue engineering. In this paper, chitosan-based composites were synthesized adding hydroxyapatite and/or magnetite in a chitosan matrix by in situ precipitation technique. Composites were characterized by optical and electron microscopy, thermogravimetric analyses (TGA), x-ray diffraction (XRD), and in vitro cell culture studies. Hydroxyapatite and magnetite were found to be homogeneously dispersed in the chitosan matrix and the composites showed superior biocompatibility and the ability to support cell attachment and proliferation; in particular, the chitosan/hydroxyapatite/magnetite composite (CS/HA/MGN) demonstrated superior bioactivity with respect to pure chitosan (CS) and to the chitosan/hydroxyapatite (CS/HA) scaffolds

The effect of surface entropy on the heat of non-wetting liquid intrusion into nanopores

On-demand access to renewable and environmentally friendly energy sources is critical to address current and future energy needs. To achieve this, the development of new mechanisms of efficient thermal energy storage (TES) is important to improve the overall energy storage capacity. Demonstrated here is the ideal concept that the thermal effect of developing a solid−liquid interface between a non-wetting liquid and hydrophobic nanoporous material can store heat to supplement current TES technologies. The fundamental macroscopic property of a liquid’s surface entropy and its relationship to its solid surface are one of the keys to predict the magnitude of the thermal effect by the development of the liquid−solid interface in a nanoscale nvironment driven through applied pressure. Demonstrated here is this correlation of these properties with the direct measurement of the thermal effect of non-wetting liquids intruding into hydrophobic nanoporous materials. It is shown that the model can resonably predict the heat of intrusion into rigid mesoporous silica and some microporous zeolite when the temperature dependence of the contact angle is applied. Conversely, intrusion into flexible microporous metal−organic frameworks requires further improvement. The reported results with further development have the potential to lead to the development of a new supplementary method and mechanim for TES